| class name | count |
|---|---|
| rosids | 34 |
| asterids | 11 |
| Spermatophyta | 6 |
| eudicotyledons | 5 |
| Liliopsida | 2 |
| Magnoliophyta | 1 |
| class name | count |
|---|---|
|
Fabaceae
|
27 |
|
Apocynaceae
|
5 |
|
Taxaceae
|
4 |
|
Viscaceae
|
2 |
|
Sapotaceae
|
2 |
|
Zingiberaceae
|
1 |
|
Solanaceae
|
1 |
|
Boraginaceae
|
1 |
|
Brassicaceae
|
1 |
|
Achariaceae
|
1 |
|
Pinaceae
|
1 |
|
Proteaceae
|
1 |
|
Magnoliaceae
|
1 |
|
Nyctaginaceae
|
1 |
|
Euphorbiaceae
|
1 |
|
Fagaceae
|
1 |
|
Arecaceae
|
1 |
|
Myrtaceae
|
1 |
|
Cupressaceae
|
1 |
|
Rutaceae
|
1 |
| br08003 Category | # of metabolite |
|---|
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| O75496 | Geminin | Unclassified protein | C00001157 C00001164 C00001166 C00001168 C00001169 C00001172 C00040932 C00048928 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00001157 C00001166 C00001168 C00001169 C00001172 C00040932 C00048928 | 1 / 1 |
| P10323 | Acrosin | S1A | C00001164 | 0 / 0 |
| P02545 | Prelamin-A/C | Unclassified protein | C00001164 | 11 / 10 |
| P16278 | Beta-galactosidase | Enzyme | C00001164 | 4 / 6 |
| P06280 | Alpha-galactosidase A | Enzyme | C00001164 | 1 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001164 | 0 / 0 |
| O43451 | Maltase-glucoamylase, intestinal | Hydrolase | C00001164 | 0 / 0 |
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00001164 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #301500 | Fabry disease |
P06280
|
| #230500 | Gm1-gangliosidosis, type i |
P16278
|
| #230600 | Gm1-gangliosidosis, type ii |
P16278
|
| #230650 | Gm1-gangliosidosis, type iii |
P16278
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #253010 | Mucopolysaccharidosis type ivb |
P16278
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
| KEGG | name | UniProt |
|---|---|---|
| H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
| H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
| H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
| H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
| H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
| H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
| H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
| H00663 | Restrictive dermopathy |
P02545
(related)
|
| H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
| H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00123 | Mucopolysaccharidosis type IV (MPS4) |
P16278
(related)
|
| H00276 | Galactosialidosis |
P16278
(related)
|
| H00281 | GM1 gangliosidosis |
P16278
(related)
|
| H00421 | Mucopolysaccharidosis (MPS) |
P16278
(related)
|
| H00422 | Glycoproteinoses |
P16278
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P16278
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|